A Ferrous sulfate, dried DMF (Drug Master File) is a document detailing the whole manufacturing process of Ferrous sulfate, dried active pharmaceutical ingredient (API) in detail. Different forms of Ferrous sulfate, dried DMFs exist exist since differing nations have different regulations, such as Ferrous sulfate, dried USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ferrous sulfate, dried DMF submitted to regulatory agencies in the US is known as a USDMF. Ferrous sulfate, dried USDMF includes data on Ferrous sulfate, dried's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ferrous sulfate, dried USDMF is kept confidential to protect the manufacturer’s intellectual property.
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